MX2017012367A - Alignment and variant sequencing analysis pipeline. - Google Patents
Alignment and variant sequencing analysis pipeline.Info
- Publication number
- MX2017012367A MX2017012367A MX2017012367A MX2017012367A MX2017012367A MX 2017012367 A MX2017012367 A MX 2017012367A MX 2017012367 A MX2017012367 A MX 2017012367A MX 2017012367 A MX2017012367 A MX 2017012367A MX 2017012367 A MX2017012367 A MX 2017012367A
- Authority
- MX
- Mexico
- Prior art keywords
- amplification
- sequence
- ngs
- solid
- alignment
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6869—Methods for sequencing
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
- C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06N—COMPUTING ARRANGEMENTS BASED ON SPECIFIC COMPUTATIONAL MODELS
- G06N3/00—Computing arrangements based on biological models
- G06N3/12—Computing arrangements based on biological models using genetic models
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06N—COMPUTING ARRANGEMENTS BASED ON SPECIFIC COMPUTATIONAL MODELS
- G06N5/00—Computing arrangements using knowledge-based models
- G06N5/04—Inference or reasoning models
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B20/00—ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
- G16B20/20—Allele or variant detection, e.g. single nucleotide polymorphism [SNP] detection
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
- G16B30/10—Sequence alignment; Homology search
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
- G16B30/20—Sequence assembly
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2535/00—Reactions characterised by the assay type for determining the identity of a nucleotide base or a sequence of oligonucleotides
- C12Q2535/122—Massive parallel sequencing
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Biophysics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Biotechnology (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Theoretical Computer Science (AREA)
- Genetics & Genomics (AREA)
- Immunology (AREA)
- General Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Bioinformatics & Computational Biology (AREA)
- Evolutionary Biology (AREA)
- Medical Informatics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Microbiology (AREA)
- Pathology (AREA)
- Biochemistry (AREA)
- Oncology (AREA)
- Hospice & Palliative Care (AREA)
- Software Systems (AREA)
- Artificial Intelligence (AREA)
- Computational Linguistics (AREA)
- Data Mining & Analysis (AREA)
- Computing Systems (AREA)
- Mathematical Physics (AREA)
- General Physics & Mathematics (AREA)
- Evolutionary Computation (AREA)
- Biomedical Technology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
Provided are systems and methods for analyzing genetic sequence data from next generation sequence (NGS) platforms. Also provided are methods for the preparation of samples for nucleic acid sequence analysis by NGS. Variant calling is performed with a modified GATK variant caller. Mapping the reads to a genomic reference sequence is performed with a Burrows Wheeler Aligner (BWA) and does not comprise soft clipping. The genomic reference sequence is GRCh37.1 human genome reference. The sequencing method comprises emulsion PCR (emPCR), rolling circle amplification, or solid-phase amplification. In some embodiments, the solid-phase amplification is clonal bridge amplification.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201562138620P | 2015-03-26 | 2015-03-26 | |
US201562253908P | 2015-11-11 | 2015-11-11 | |
PCT/US2016/024319 WO2016154584A1 (en) | 2015-03-26 | 2016-03-25 | Alignment and variant sequencing analysis pipeline |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2017012367A true MX2017012367A (en) | 2017-12-14 |
Family
ID=56978583
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2017012367A MX2017012367A (en) | 2015-03-26 | 2016-03-25 | Alignment and variant sequencing analysis pipeline. |
MX2022009242A MX2022009242A (en) | 2015-03-26 | 2017-09-26 | Alignment and variant sequencing analysis pipeline. |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2022009242A MX2022009242A (en) | 2015-03-26 | 2017-09-26 | Alignment and variant sequencing analysis pipeline. |
Country Status (8)
Country | Link |
---|---|
US (1) | US20180051329A1 (en) |
EP (1) | EP3274475A4 (en) |
CN (2) | CN116042833A (en) |
BR (1) | BR112017020363A2 (en) |
CA (1) | CA2980327A1 (en) |
HK (1) | HK1250520A1 (en) |
MX (2) | MX2017012367A (en) |
WO (1) | WO2016154584A1 (en) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9476095B2 (en) | 2011-04-15 | 2016-10-25 | The Johns Hopkins University | Safe sequencing system |
EP3447495B2 (en) | 2012-10-29 | 2024-03-13 | The Johns Hopkins University | Papanicolaou test for ovarian and endometrial cancers |
US10395759B2 (en) | 2015-05-18 | 2019-08-27 | Regeneron Pharmaceuticals, Inc. | Methods and systems for copy number variant detection |
US11286531B2 (en) | 2015-08-11 | 2022-03-29 | The Johns Hopkins University | Assaying ovarian cyst fluid |
US10600499B2 (en) | 2016-07-13 | 2020-03-24 | Seven Bridges Genomics Inc. | Systems and methods for reconciling variants in sequence data relative to reference sequence data |
US10296842B2 (en) | 2017-07-21 | 2019-05-21 | Helix OpCo, LLC | Genomic services system with dual-phase genotype imputation |
US10622095B2 (en) * | 2017-07-21 | 2020-04-14 | Helix OpCo, LLC | Genomic services platform supporting multiple application providers |
EP3665308A1 (en) | 2017-08-07 | 2020-06-17 | The Johns Hopkins University | Methods and materials for assessing and treating cancer |
WO2019079464A1 (en) | 2017-10-17 | 2019-04-25 | Jungla Inc. | Molecular evidence platform for auditable, continuous optimization of variant interpretation in genetic and genomic testing and analysis |
WO2019169304A1 (en) * | 2018-03-02 | 2019-09-06 | Mirna Analytics Llc | Biomarker detection in pulmonary hypertension |
JP6891151B2 (en) * | 2018-08-31 | 2021-06-18 | シスメックス株式会社 | Analysis method, information processing device, gene analysis system, program, recording medium |
CN109321646A (en) * | 2018-09-12 | 2019-02-12 | 山东省农作物种质资源中心 | The virtual PCR method compared based on NGS read and reference sequences |
WO2020081648A1 (en) * | 2018-10-17 | 2020-04-23 | Quest Diagnostics Investments Llc | Genomic sequencing selection system |
WO2020242603A1 (en) * | 2019-05-24 | 2020-12-03 | Qiagen Sciences Llc | Methods and usage for quantitative evaluation of clonal amplified products and sequencing qualities |
CA3162799A1 (en) * | 2019-12-23 | 2021-07-01 | Benjamin F. DELATTE | Methods and kits for the enrichment and detection of dna and rna modifications and functional motifs |
CN111243666B (en) * | 2020-01-08 | 2023-04-07 | 华南理工大学 | Nextflow-based automatic analysis method and system for circular ribonucleic acid |
KR102345994B1 (en) * | 2020-01-22 | 2022-01-03 | 가톨릭대학교 산학협력단 | Method and apparatus for screening gene related with disease in next generation sequence analysis |
EP4332975A1 (en) * | 2022-08-29 | 2024-03-06 | Siemens Healthcare Diagnostics Products GmbH | Method for eliminating non-natural sequence portions from fastq sequence data |
CN116864007B (en) * | 2023-09-05 | 2023-12-26 | 深圳人体密码基因科技有限公司 | Analysis method and system for gene detection high-throughput sequencing data |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101037690B (en) * | 2006-03-16 | 2011-07-20 | 国家人口计生委科学技术研究所 | BRCA1 gene variant having new single nucleotide polymorphism and encoded protein variant |
CN101200766B (en) * | 2007-12-24 | 2012-06-06 | 北京美康生物技术研究中心 | Multiple PCR reagent kit detecting breast cancer susceptibility gene mutation and preparation method thereof |
US20110257889A1 (en) * | 2010-02-24 | 2011-10-20 | Pacific Biosciences Of California, Inc. | Sequence assembly and consensus sequence determination |
WO2013043909A1 (en) * | 2011-09-20 | 2013-03-28 | Life Technologies Corporation | Systems and methods for identifying sequence variation |
CN102329876B (en) * | 2011-10-14 | 2014-04-02 | 深圳华大基因科技有限公司 | Method for measuring nucleotide sequence of disease associated nucleic acid molecules in sample to be detected |
US9552458B2 (en) * | 2012-03-16 | 2017-01-24 | The Research Institute At Nationwide Children's Hospital | Comprehensive analysis pipeline for discovery of human genetic variation |
WO2014152990A1 (en) * | 2013-03-14 | 2014-09-25 | University Of Rochester | System and method for detecting population variation from nucleic acid sequencing data |
US9116866B2 (en) * | 2013-08-21 | 2015-08-25 | Seven Bridges Genomics Inc. | Methods and systems for detecting sequence variants |
CN104232761A (en) * | 2014-08-27 | 2014-12-24 | 武汉凯吉盈科技有限公司 | Gene complete segment quick sequencing method |
-
2016
- 2016-03-25 CA CA2980327A patent/CA2980327A1/en active Pending
- 2016-03-25 MX MX2017012367A patent/MX2017012367A/en unknown
- 2016-03-25 CN CN202310086286.9A patent/CN116042833A/en active Pending
- 2016-03-25 US US15/560,611 patent/US20180051329A1/en active Pending
- 2016-03-25 EP EP16769805.9A patent/EP3274475A4/en active Pending
- 2016-03-25 CN CN201680030228.2A patent/CN107849612B/en active Active
- 2016-03-25 WO PCT/US2016/024319 patent/WO2016154584A1/en active Application Filing
- 2016-03-25 BR BR112017020363A patent/BR112017020363A2/en active Search and Examination
-
2017
- 2017-09-26 MX MX2022009242A patent/MX2022009242A/en unknown
-
2018
- 2018-07-31 HK HK18109881.3A patent/HK1250520A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
EP3274475A1 (en) | 2018-01-31 |
HK1250520A1 (en) | 2018-12-21 |
MX2022009242A (en) | 2022-08-18 |
WO2016154584A1 (en) | 2016-09-29 |
EP3274475A4 (en) | 2018-12-05 |
US20180051329A1 (en) | 2018-02-22 |
BR112017020363A2 (en) | 2018-06-05 |
CN107849612B (en) | 2023-04-14 |
CN107849612A (en) | 2018-03-27 |
CA2980327A1 (en) | 2016-09-29 |
CN116042833A (en) | 2023-05-02 |
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